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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973633Generated: October 31, 2026

Ethanol → HCID 21490097, compound

https://huagongshe.com/reaction/1973633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium IodideHCID 5238—
ReactantPotassium thiocyanateHCID 516872—
Reactant2-Chloro-1-(2,4,6-trimethyl-1-piperidinyl)ethanoneHCID 21490080—
SolventBenzeneHCID 241—
ProductHCID 21490097HCID 21490097—

Reaction Steps

1-(α-Chloroacetyl)-2,4,6-trimethylpiperidine (18 grams; 0.9 mol), potassium thiocyanate (18 grams; 0.2 mol), sodium iodide (a few crystals) and ethanol (100 ml) were charged into a glass reaction flask equipped with a mechanical stirrer and reflux condenser. The reaction mixture was heated at reflux for a period of about 3 hours. After this time the mixture was cooled and filtered. The filtrate was evaporated leaving a solid product. The solid was then extracted with two 150 ml portions of hot benzene. The extracts were combined and evaporated under reduced pressure to yield an oil. This oil was refined by chromatography using Fuller's earth as an adsorbent and benzene as the elluent. The first 1000 ml of eluent were collected from the column and were stripped of benzene to yield 1-(α-thiocyanoacetyl)-2,4,6-trimethylpiperidine as a yellow oil having a refractive index of 1.5183 at 25° C. and having the following elemental analysis as calculated for C11H18N2OS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998808
Source datasetuspto-grants-1976_12
ORD IDord-086179aea5304d98a68949e8f23869bb
Source noteuspto-grants-1976_12